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[3,3'-Bipyridine]-2,2'-diamine, with the molecular formula C12H12N4, is a chemical compound that is a diamine derivative of 3,3'-bipyridine. It features two pyridine rings connected by a carbon-carbon bond and is known for its ability to chelate metal ions, making it a versatile ligand in various applications.

77200-37-4

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77200-37-4 Usage

Uses

Used in Coordination Chemistry and Metal-Organic Frameworks:
[3,3'-Bipyridine]-2,2'-diamine is used as a versatile ligand for the formation of metal complexes in coordination chemistry and metal-organic frameworks. Its unique structure and nitrogen-containing functional groups enable the creation of stable complexes with a wide range of metal ions.
Used in Catalysis:
In the field of catalysis, [3,3'-Bipyridine]-2,2'-diamine is used as a ligand in the development of catalysts for various chemical reactions. Its ability to chelate metal ions allows for the creation of active and selective catalysts that can improve the efficiency and selectivity of these reactions.
Used in Sensing:
[3,3'-Bipyridine]-2,2'-diamine is employed as a sensing agent in the development of chemical sensors. Its interaction with metal ions can be exploited to create sensors that can detect and quantify specific analytes, making it a valuable component in the field of analytical chemistry.
Used in Material Science:
In material science, [3,3'-Bipyridine]-2,2'-diamine is used as a building block for the synthesis of new materials with unique properties. Its ability to form stable complexes with metal ions can lead to the development of materials with enhanced mechanical, electrical, or optical properties.
Used in Pharmaceutical Applications:
[3,3'-Bipyridine]-2,2'-diamine has potential pharmaceutical applications, particularly in the development of metal-based anticancer drugs. Its ability to chelate metal ions can be utilized to create drugs with improved efficacy and reduced side effects, making it a promising candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 77200-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,0 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77200-37:
(7*7)+(6*7)+(5*2)+(4*0)+(3*0)+(2*3)+(1*7)=114
114 % 10 = 4
So 77200-37-4 is a valid CAS Registry Number.

77200-37-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-aminopyridin-3-yl)pyridin-2-amine

1.2 Other means of identification

Product number -
Other names <3,3'-bibyridine>-2,2'-diamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:77200-37-4 SDS

77200-37-4Relevant academic research and scientific papers

A Convenient Synthetic Route to bis-Heteroaromatic and bis-Heterocyclic Compounds Promoted by Liganded Nickel Complex Reducing Agents.

Forst, Yves,Becker, Sandrine,Caubere, Paul

, p. 11893 - 11902 (2007/10/02)

A number of nitrogen, sulfur or oxygen containing bis-heteroaromatic or bis-heterocyclic derivatives have been synthesized in good to excellent yields by homocoupling of the corresponding halogenated compounds in the presence of liganded (triphenylphosphine or 2,2'-bipyridine) nickel Complex Reducing Agents in THF or DME at 63 deg C.

Bipyridines. Part XV. A Novel Convenient Synthesis of Some 3,3'-Bipyridine Derivatives

Becalski, Adam,Kaczmarek, Lukasz,Nantka-Namirski, Pawel

, p. 105 - 114 (2007/10/02)

A new, convenient synthesis of 2,2'-dinitro-(10), 4,4'-dinitro-(11), 1,1'-dioxo-4,4'-dinitro- (12) and 2,2'-dioxo- (13) -3,3'-bipyridines by aplication of the Ullmann reaction is reported.The possibility of the nitro-groups substitution by such nucleophil

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